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Beckman Coulter Reticulated Red Blood Cell Treatment (Non-sterile) - Taiwan Registration 9843607c6e63c9b1affd9c86656dbbe9

Access comprehensive regulatory information for Beckman Coulter Reticulated Red Blood Cell Treatment (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9843607c6e63c9b1affd9c86656dbbe9 and manufactured by Beckman Coulter, Inc.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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9843607c6e63c9b1affd9c86656dbbe9
Registration Details
Taiwan FDA Registration: 9843607c6e63c9b1affd9c86656dbbe9
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Device Details

Beckman Coulter Reticulated Red Blood Cell Treatment (Non-sterile)
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น ็ถฒ็‹€็ด…่ก€็ƒ่™•็†ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

9843607c6e63c9b1affd9c86656dbbe9

DHA084A0031700

Company Information

United States

Product Details

It is limited to the first-level identification scope of medical device classification and grading management of distinguishing dyes and chemical solution dyes (B.1850).

B Hematology, pathology, and genetics

B.1850 Dyes and dyes for chemical solutions

import

Dates and Status

Nov 14, 2024

Oct 31, 2026